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API SUPPLIERS
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USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Faran Shimi Pharmaceutical
Faran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.
Dosage Form : Tablet
Grade : Oral
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Healthcare
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Shenmei Pharmaceutical Technology Co., Ltd
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ABOUT THIS PAGE
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PharmaCompass offers a list of Aluminum Magnesium Silicate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Aluminum Magnesium Silicate manufacturer or Aluminum Magnesium Silicate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aluminum Magnesium Silicate manufacturer or Aluminum Magnesium Silicate supplier.
PharmaCompass also assists you with knowing the Aluminum Magnesium Silicate API Price utilized in the formulation of products. Aluminum Magnesium Silicate API Price is not always fixed or binding as the Aluminum Magnesium Silicate Price is obtained through a variety of data sources. The Aluminum Magnesium Silicate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Veegum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Veegum, including repackagers and relabelers. The FDA regulates Veegum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Veegum API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Veegum supplier is an individual or a company that provides Veegum active pharmaceutical ingredient (API) or Veegum finished formulations upon request. The Veegum suppliers may include Veegum API manufacturers, exporters, distributors and traders.
click here to find a list of Veegum suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Veegum DMF (Drug Master File) is a document detailing the whole manufacturing process of Veegum active pharmaceutical ingredient (API) in detail. Different forms of Veegum DMFs exist exist since differing nations have different regulations, such as Veegum USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Veegum DMF submitted to regulatory agencies in the US is known as a USDMF. Veegum USDMF includes data on Veegum's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Veegum USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Veegum suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Veegum Drug Master File in Japan (Veegum JDMF) empowers Veegum API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Veegum JDMF during the approval evaluation for pharmaceutical products. At the time of Veegum JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Veegum suppliers with JDMF on PharmaCompass.
Veegum Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Veegum GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Veegum GMP manufacturer or Veegum GMP API supplier for your needs.
A Veegum CoA (Certificate of Analysis) is a formal document that attests to Veegum's compliance with Veegum specifications and serves as a tool for batch-level quality control.
Veegum CoA mostly includes findings from lab analyses of a specific batch. For each Veegum CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Veegum may be tested according to a variety of international standards, such as European Pharmacopoeia (Veegum EP), Veegum JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Veegum USP).
